Browsing: Huntingtion’s Disease

Huntington’s disease is a progressive neurodegenerative disorder caused by a genetic mutation in the HTT gene, leading to the gradual breakdown of nerve cells in the brain. This inherited condition typically manifests in mid-adulthood and is characterized by a combination of motor, cognitive, and psychiatric symptoms. Individuals with Huntington’s disease experience involuntary movements (chorea), difficulties with coordination and balance, as well as cognitive decline, including impaired judgment and memory. The disease also leads to emotional and behavioral changes, such as depression, irritability, and anxiety. Huntington’s disease is currently incurable, and treatment focuses on managing symptoms and improving the quality of life for those affected.